BEUDAMED
    183 results · 22ms · Sources: EU EUDAMED, US FDA

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    Monitor, Carbon-Dioxide, Cutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·CUTANIOUS GAS MONITOR

    Monitor, Carbon-Dioxide, Cutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·CUTANIOUS GAS MONITOR

    Monitor, Carbon-Dioxide, Cutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·CUTANIOUS GAS MONITOR

    Axcent Acrylics

    FDA UDI
    GARRECO, LLC·D79338300080·ACR MON #3 SC (8 OZ EACH)

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707028215·WEB 1ST MOLAR BANDS n.UL 8

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88300081·Max. 1. Molar band W-Fit right 08

    NTI

    FDA UDI
    NTI - Kahla GmbH Rotary Dental Instruments·E310830008MFG1·NTI Diamond Medium FG

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88300080101·Max. 1. Molar band W-Fit right 08

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88300080051·Max. 1. Molar band W-Fit right 08

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88300080501·Max. 1. Molar band W-Fit right 08

    KARICKHOFF KERATOSCOPE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Stimulator, Hypoglossal Nerve, Implanted, Apnea

    FDA Pre-Market Approval
    FDA Class 3 ·INSPIRE II UPPER AIRWAY STIMULATOR

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·WAVELIGHT ALLEGRETTO WAVE EXCIMER LASER SYSTEM

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·May 23, 2014

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·November 13, 2012

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 3, 2010

    Stimulator, Hypoglossal Nerve, Implanted, Apnea

    FDA Pre-Market Approval
    FDA Class 3 ·Model 4063 Inspire Stimulation Lead, Model 4340 Inspire Sensing Lead

    Stimulator, Hypoglossal Nerve, Implanted, Apnea

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 3150 IMPLANTABLE PULSE GENERATOR (IPG)

    Stimulator, Hypoglossal Nerve, Implanted, Apnea

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 3024 INSPIRE II IMPLANTABLE PULSE GENERATOR (IPG)

    Stimulator, Hypoglossal Nerve, Implanted, Apnea

    FDA Pre-Market Approval
    FDA Class 3 ·Inspire Model 3028 Implantable Pulse Generator (IPG)